Melanins (eumelanins, pheomelanins) are photoprotective pigments. They remove light energy, dissipating it either as heat or in a chemical reaction in which oxygen is consumed. Recent work has shown that they also scavenge toxic species, e.g. superoxide and singlet oxygen. Protection may arise either from light filtering, removal of oxygen, or such scavenging. The cost of the protection is measured in terms of the chemical or thermal damage that may result. If the damage outweighs the protection afforded by the pigment, phototoxicity results: it has been hypothesized that damage may be more pronounced with pheomelanins than with eumelanins and may promote skin cancer in red-haired individuals. New experiments are proposed to: (i) measure the effectiveness of isolated pigments in scavenging superoxide and singlet oxygen and the resulting damage to the melanin (e.g. bleaching, irreversible free-radical production); (ii) determine whether scavenging reactions are effective in melanosomal and cellular systems; (iii) determine the effect of melanin on cell respiration and survival following exposure either to visible or UV light in the absence or presence of sensitizers. These experiments will include a comparison of eumelanins and pheomelanins, and an assessment of the utility of sensitizers in promoting chemical or thermal damage in pigmented cells will be made. In these studies use will be made of recently-developed electron spin resonance (ESR) procedures for measuring oxygen consumption and superoxide production in photolytic and cellular systems and of a new model pigmented cell system: Chinese hamster ovary (CHO) cells containing phagocytized melanin.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis, Diabetes, Digestive and Kidney Diseases (NIADDK)
Type
Research Project (R01)
Project #
5R01AM026950-06
Application #
3151689
Study Section
Biophysics and Biophysical Chemistry A Study Section (BBCA)
Project Start
1980-08-01
Project End
1986-07-31
Budget Start
1985-08-01
Budget End
1986-07-31
Support Year
6
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Medical College of Wisconsin
Department
Type
Schools of Medicine
DUNS #
073134603
City
Milwaukee
State
WI
Country
United States
Zip Code
53226
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Kalyanaraman, B; Feix, J B; Sieber, F et al. (1987) Photodynamic action of merocyanine 540 on artificial and natural cell membranes: involvement of singlet molecular oxygen. Proc Natl Acad Sci U S A 84:2999-3003
Menon, I A; Basu, P K; Persad, S et al. (1987) Is there any difference in the photobiological properties of melanins isolated from human blue and brown eyes? Br J Ophthalmol 71:549-52
Korytowski, W; Pilas, B; Sarna, T et al. (1987) Photoinduced generation of hydrogen peroxide and hydroxyl radicals in melanins. Photochem Photobiol 45:185-90
Pilas, B; Felix, C C; Sarna, T et al. (1986) Photolysis of pheomelanin precursors: an ESR-spin trapping study. Photochem Photobiol 44:689-96
Ankel, E; Felix, C C; Kalyanaraman, B (1986) The use of spin label oximetry in the study of photodynamic inactivation of Chinese hamster ovary cells. Photochem Photobiol 44:741-6
Hintz, P; Kalyanaraman, B (1986) Metal ion-induced activation of molecular oxygen in pigmented polymers. Biochim Biophys Acta 883:41-5
Korytowski, W; Kalyanaraman, B; Menon, I A et al. (1986) Reaction of superoxide anions with melanins: electron spin resonance and spin trapping studies. Biochim Biophys Acta 882:145-53
Sarna, T; Korytowski, W; Sealy, R C (1985) Nitroxides as redox probes of melanins: dark-induced and photoinduced changes in redox equilibria. Arch Biochem Biophys 239:226-33
Sarna, T; Menon, I A; Sealy, R C (1985) Photosensitization of melanins: a comparative study. Photochem Photobiol 42:529-32

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